Figure 4
Figure 4. BM hypoplasia and stem cell impairment in agrin-deficient (Musk-L;Agrn−/−) mice. (A) Representative flow cytometric analysis of the LSK population for control and Musk-L;Agrn−/− mice and mean numbers relative to controls are shown. Dot plots correspond to the Lin−/IL7R− gate and the indicated values represent the percentage among total BM cells (ctrl, n = 26; Musk-L;Agrn−/−, n = 11; *P < .05). (B) Representative flow cytometric analysis on LSK population: the analysis of CD150 versus CD41/48 expression and the analysis of CD135 versus CD34 expression were done on the Lin−IL7R−c-Kit+Sca-1+ population; the indicated values represent the percentage among total LSK cells. Pie charts represent average frequencies of the 3 subsets within LSK population (ctrl, n = 6; Musk-L;Agrn−/−, n = 4;). CD150+CD41/48− LSK and CD34+CD135− LSK population frequencies are statistically different (P < .05). (C) Annexin V (top row) and cleaved caspase-3 (bottom row) analysis on CD34+CD135− LSK cells. Left, representative flow cytometry profiles; right, statistical analysis (annexin: ctrl, n = 6; Musk-L;Agrn−/−, n = 4; cleaved caspase-3: ctrl, n = 5; Musk-L;Agrn−/−, n = 3; **P < .01). (D) Mean numbers relative to controls of the hematopoietic progenitors for control and Musk-L;Agrn−/− mice are shown. CMPs are defined as Lin−IL7R−Sca-1−c-Kit+CD34+CD16/32low, GMPs as Lin−IL7R−Sca-1−c-Kit+ CD34+CD16/32+, MEPs as Lin−IL7R−Sca-1−c-Kit+CD34−CD16/32−, and CLPs are defined as Lin−IL7R+Sca-1loc-Kit+ (ctrl, n = 15; Musk-L;Agrn−/−, n = 8; *P < .05). In all panels, error bars represent SEM.

BM hypoplasia and stem cell impairment in agrin-deficient (Musk-L;Agrn−/−) mice. (A) Representative flow cytometric analysis of the LSK population for control and Musk-L;Agrn−/− mice and mean numbers relative to controls are shown. Dot plots correspond to the Lin/IL7R gate and the indicated values represent the percentage among total BM cells (ctrl, n = 26; Musk-L;Agrn−/−, n = 11; *P < .05). (B) Representative flow cytometric analysis on LSK population: the analysis of CD150 versus CD41/48 expression and the analysis of CD135 versus CD34 expression were done on the LinIL7Rc-Kit+Sca-1+ population; the indicated values represent the percentage among total LSK cells. Pie charts represent average frequencies of the 3 subsets within LSK population (ctrl, n = 6; Musk-L;Agrn−/−, n = 4;). CD150+CD41/48 LSK and CD34+CD135 LSK population frequencies are statistically different (P < .05). (C) Annexin V (top row) and cleaved caspase-3 (bottom row) analysis on CD34+CD135 LSK cells. Left, representative flow cytometry profiles; right, statistical analysis (annexin: ctrl, n = 6; Musk-L;Agrn−/−, n = 4; cleaved caspase-3: ctrl, n = 5; Musk-L;Agrn−/−, n = 3; **P < .01). (D) Mean numbers relative to controls of the hematopoietic progenitors for control and Musk-L;Agrn−/− mice are shown. CMPs are defined as LinIL7RSca-1c-Kit+CD34+CD16/32low, GMPs as LinIL7RSca-1c-Kit+ CD34+CD16/32+, MEPs as LinIL7RSca-1c-Kit+CD34CD16/32, and CLPs are defined as LinIL7R+Sca-1loc-Kit+ (ctrl, n = 15; Musk-L;Agrn−/−, n = 8; *P < .05). In all panels, error bars represent SEM.

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